The human and African green monkey TRIM5α genes encode Ref1 and Lv1 retroviral restriction factor activities

  1. Zuzana Keckesova,
  2. Laura M. J. Ylinen, and
  3. Greg J. Towers*
  1. Wohl Virion Center, Division of Infection and Immunity, University College London, London W1T 4JF, United Kingdom
  1. Edited by John M. Coffin, Tufts University School of Medicine, Boston, MA (received for review April 7, 2004)

Abstract

The rhesus macaque tripartite motif containing protein TRIM5α specifically restricts HIV-1 infection at an early post-entry step before reverse transcription [Stremlau, M., Owens, C. M., Perron, M. J., Kiessling, M., Autissier, P. & Sodroski, J. (2004) Nature 427, 848–853]. Here, we show that the human and African green monkey (AGM) TRIM5α genes encode Ref1 and Lv1 antiretroviral activities, respectively. Expression of TRIM5α in permissive cat cells renders them resistant to restriction-sensitive murine leukemia virus but not closely related insensitive virus. Disruption of TRIM5α expression in human and AGM cells with small interfering RNA rescues infectivity of restricted virus without affecting unrestricted virus. We also demonstrate that the activity of the murine restriction factor Fv1 depends on TRIM5α expression when Fv1 is expressed in human cells. Furthermore, a drug that modifies the behavior of the related promyelocytic leukemia protein PML specifically rescues infection by viruses restricted by human TRIM5α. Alignment of the TRIM5α proteins from rhesus macaque and AGM indicates an 18-aa insertion. We speculate that this insertion may contribute to the broader specificity of the AGM TRIM5α restriction as compared with the human and rhesus macaque proteins.

Footnotes

  • * To whom correspondence should be addressed at: Wohl Virion Center, Windeyer Building, University College London, 46 Cleveland Street, London W1T 4JF, United Kingdom. E-mail: g.towers{at}ucl.ac.uk.

  • This paper was submitted directly (Track II) to the PNAS office.

  • Abbreviations: AGM, African green monkey; MLV, murine leukemia virus; EIAV, equine infectious anemia virus; RFP, red fluorescent protein; FACS, fluorescence-activated cell sorter; CA, capsid; MDTF, Mus dunni tail fibroblasts; siRNA, small interfering RNA; PML, promyelocytic leukemia.

  • Data deposition: The sequence reported in this paper has been deposited in the GenBank database (accession no. AY593973).

  • See Commentary on page 10496.

« Previous | Next Article »Table of Contents